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Serum neurofilament light chain levels in patients with cognitive deficits and movement disorders:comparison of cerebrospinal and serum neurofilament light chain levels with other biomarkers

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F23%3AE0110562" target="_blank" >RIV/00843989:_____/23:E0110562 - isvavai.cz</a>

  • Alternative codes found

    RIV/61988987:17110/23:A2402NOS

  • Result on the web

    <a href="https://www.frontiersin.org/articles/10.3389/fnhum.2023.1284416/full?&utm_source=Email_to_authors_&utm_medium=Email&utm_content=T1_11.5e1_author&utm_campaign=Email_publication&field=&journalName=Frontiers_in_Human_Neuroscience&id=1284416" target="_blank" >https://www.frontiersin.org/articles/10.3389/fnhum.2023.1284416/full?&utm_source=Email_to_authors_&utm_medium=Email&utm_content=T1_11.5e1_author&utm_campaign=Email_publication&field=&journalName=Frontiers_in_Human_Neuroscience&id=1284416</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3389/fnhum.2023.1284416" target="_blank" >10.3389/fnhum.2023.1284416</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Serum neurofilament light chain levels in patients with cognitive deficits and movement disorders:comparison of cerebrospinal and serum neurofilament light chain levels with other biomarkers

  • Original language description

    Background: Serum neurofilament light chain (S NfL) is a non-specific marker of neuronal damage, including Alzheimer’s disease (AD). We aimed to verify the reference interval (RI) of serum NfL using a highly sensitive ELISA, and to estimate the optimal cut-off value for neuronal damage. Our second objective was to compare NfL in cerebrospinal fluid (CSF) and serum (S) with the routine neurodegeneration biomarkers used in AD, and to assess their concentrations relative to the degree of cognitive deficit. Methods: Samples from 124 healthy volunteers were used to estimate the S NfL RI. For the comparison study, we used CSF and S samples from 112 patients with cognitive disorders. Cognitive functions were assessed using the mini-mental state examination. ELISA assays were used to determine the CSF and S NfL levels, CSF ß-amyloid peptide42 (Aß42), CSF ß-amyloid peptide40 (Aß40), CSF total tau protein (tTau), CSF phosphorylated tau protein (pTau), and CSF alpha-synuclein (?S). Results: The estimated RI of S NfL were 2.25–9.19 ng.L–1. The cut-off value of S NfL for assessing the degree of neuronal impairment was 10.5 ng.L–1. We found a moderate statistically significant correlation between S NfL and CSF Aß42 in the group with movement disorders, without dementia (rs = 0.631; p = 0.016); between S NfL and CSF Aß40 in the group with movement disorder plus dementia (rs = -0.750; p = 0.052); between S NfL and CSF tTau in the control group (rs = 0.689; p = 0.009); and between S NfL and CSF pTau in the control group (rs = 0.749; p = 0.003). The non-parametric Kruskal–Wallis test revealed statistically significant differences between S NfL, CSF NfL, CSF Aß42, CSF tTau, and CSF pTau and diagnosis within groups. The highest kappa coefficients were found between the concentrations of S NfL and CSF NfL (? = 0.480) and between CSF NfL and CSF tTau (? = 0.351). Conclusion: Our results suggested that NfL and tTau in CSF of patients with cognitive decline could be replaced by the less...

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30210 - Clinical neurology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Frontiers in human neuroscience

  • ISSN

    1662-5161

  • e-ISSN

    1662-5161

  • Volume of the periodical

    17

  • Issue of the periodical within the volume

    article 1284416

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    11

  • Pages from-to

    1-11

  • UT code for WoS article

    001131708300001

  • EID of the result in the Scopus database

    2-s2.0-85180881475